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p53R2 as a novel prognostic biomarker in nasopharyngeal carcinoma
BACKGROUND: p53R2 is a target of p53 gene, which is essential for DNA repair, mitochondrial DNA synthesis, protection against oxidative stress, chromosomal instability, chronic inflammation and tumorigenesis. This study is aimed to investigate the expression of ribonucleotide reductase (RR) subunit...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5729457/ https://www.ncbi.nlm.nih.gov/pubmed/29237424 http://dx.doi.org/10.1186/s12885-017-3858-4 |
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author | Chen, Jiewei Li, Shuman Xiao, Yongbo Zou, Xuan Zhang, Xinke Zhu, Mingshu Cai, Muyan Xie, Dan |
author_facet | Chen, Jiewei Li, Shuman Xiao, Yongbo Zou, Xuan Zhang, Xinke Zhu, Mingshu Cai, Muyan Xie, Dan |
author_sort | Chen, Jiewei |
collection | PubMed |
description | BACKGROUND: p53R2 is a target of p53 gene, which is essential for DNA repair, mitochondrial DNA synthesis, protection against oxidative stress, chromosomal instability, chronic inflammation and tumorigenesis. This study is aimed to investigate the expression of ribonucleotide reductase (RR) subunit p53R2 in nasopharyngeal carcinoma and its significance in the prognosis. METHODS: The expression levels of p53R2 in 201 patients with NPC were examined by immunohistochemical assay. The correlations of p53R2 expression and clinicopathological features of nasopharyngeal carcinoma patient were analysed by chi-square test. The Kaplan-Meier survival analysis and Cox multivariate regression model were used to analyze the prognostic significance of the patients with NPC. RESULTS: Immunohistochemical results showed that p53R2 was positively expressed in 92.5% (186/201) of nasopharyngeal carcinoma and the high expression rate was 38.3% (77/201). Further analysis observed that the negative correlation between expression of p53R2 and pT status had statistical significance (P < 0.05). Kaplan-Meier survival analysis found that the mean survival time of patients with high expression of p53R2 was 143.32 months, while the patients with low expression level of p53R2 was 121.63 months (P < 0.05). Cox regression analysis suggested that p53R2 protein expression could be used as an independent prognostic factor for nasopharyngeal carcinoma (P < 0.05). CONCLUSIONS: This study drew a conclusion that p53R2 could be used as a prognostic biomarker indicative of the favorable outcome for patients with nasopharyngeal carcinoma. |
format | Online Article Text |
id | pubmed-5729457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57294572017-12-18 p53R2 as a novel prognostic biomarker in nasopharyngeal carcinoma Chen, Jiewei Li, Shuman Xiao, Yongbo Zou, Xuan Zhang, Xinke Zhu, Mingshu Cai, Muyan Xie, Dan BMC Cancer Research Article BACKGROUND: p53R2 is a target of p53 gene, which is essential for DNA repair, mitochondrial DNA synthesis, protection against oxidative stress, chromosomal instability, chronic inflammation and tumorigenesis. This study is aimed to investigate the expression of ribonucleotide reductase (RR) subunit p53R2 in nasopharyngeal carcinoma and its significance in the prognosis. METHODS: The expression levels of p53R2 in 201 patients with NPC were examined by immunohistochemical assay. The correlations of p53R2 expression and clinicopathological features of nasopharyngeal carcinoma patient were analysed by chi-square test. The Kaplan-Meier survival analysis and Cox multivariate regression model were used to analyze the prognostic significance of the patients with NPC. RESULTS: Immunohistochemical results showed that p53R2 was positively expressed in 92.5% (186/201) of nasopharyngeal carcinoma and the high expression rate was 38.3% (77/201). Further analysis observed that the negative correlation between expression of p53R2 and pT status had statistical significance (P < 0.05). Kaplan-Meier survival analysis found that the mean survival time of patients with high expression of p53R2 was 143.32 months, while the patients with low expression level of p53R2 was 121.63 months (P < 0.05). Cox regression analysis suggested that p53R2 protein expression could be used as an independent prognostic factor for nasopharyngeal carcinoma (P < 0.05). CONCLUSIONS: This study drew a conclusion that p53R2 could be used as a prognostic biomarker indicative of the favorable outcome for patients with nasopharyngeal carcinoma. BioMed Central 2017-12-13 /pmc/articles/PMC5729457/ /pubmed/29237424 http://dx.doi.org/10.1186/s12885-017-3858-4 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Chen, Jiewei Li, Shuman Xiao, Yongbo Zou, Xuan Zhang, Xinke Zhu, Mingshu Cai, Muyan Xie, Dan p53R2 as a novel prognostic biomarker in nasopharyngeal carcinoma |
title | p53R2 as a novel prognostic biomarker in nasopharyngeal carcinoma |
title_full | p53R2 as a novel prognostic biomarker in nasopharyngeal carcinoma |
title_fullStr | p53R2 as a novel prognostic biomarker in nasopharyngeal carcinoma |
title_full_unstemmed | p53R2 as a novel prognostic biomarker in nasopharyngeal carcinoma |
title_short | p53R2 as a novel prognostic biomarker in nasopharyngeal carcinoma |
title_sort | p53r2 as a novel prognostic biomarker in nasopharyngeal carcinoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5729457/ https://www.ncbi.nlm.nih.gov/pubmed/29237424 http://dx.doi.org/10.1186/s12885-017-3858-4 |
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